rs876659158

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AAGGT;AAGGT)	0	common in clinvar

Make rs876659158(-;-)

Make rs876659158(-;GTAAG)

Make rs876659158(GTAAG;GTAAG)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132605000

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs876659158
dbSNP (classic)	rs876659158
ClinGen	rs876659158
ebi	rs876659158
HLI	rs876659158
Exac	rs876659158
Gnomad	rs876659158
Varsome	rs876659158
LitVar	rs876659158
Map	rs876659158
PheGenI	rs876659158
Biobank	rs876659158
1000 genomes	rs876659158
hgdp	rs876659158
ensembl	rs876659158
geneview	rs876659158
scholar	rs876659158
google	rs876659158
pharmgkb	rs876659158
gwascentral	rs876659158
openSNP	rs876659158
23andMe	rs876659158
SNPshot	rs876659158
SNPdbe	rs876659158
MSV3d	rs876659158
GWAS Ctlg	rs876659158

Max Magnitude

0

ClinVar
Risk	rs876659158(-;-)
Alt	rs876659158(-;-)
Reference	Rs876659158(AAGGT;AAGGT)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131940692_131940696delGTAAG
CLNSRC
CLNACC	RCV000220659.1,